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FDA 510(k)

EPW POWERED WHEELCHAIR, GP-201

K-Number: K023148 · 2003-01-24

ApplicantEmg Technology Co., Ltd.
Decision Date2003-01-24
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

EPW POWERED WHEELCHAIR, GP-201 is the device name listed in this FDA 510(k) record. The listed applicant is Emg Technology Co., Ltd.. It received FDA 510(k) clearance on 2003-01-24 under 510(k) number K023148. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EPW POWERED WHEELCHAIR, GP-201?

EPW POWERED WHEELCHAIR, GP-201 is a medical device that received FDA 510(k) clearance on 2003-01-24. The listed applicant is Emg Technology Co., Ltd.. The 510(k) number is K023148.

When did EPW POWERED WHEELCHAIR, GP-201 receive FDA 510(k) clearance?

EPW POWERED WHEELCHAIR, GP-201 received FDA 510(k) clearance on 2003-01-24, under 510(k) number K023148.

Who is the listed applicant for EPW POWERED WHEELCHAIR, GP-201?

The FDA 510(k) record lists Emg Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EPW POWERED WHEELCHAIR, GP-201?

The FDA product code for EPW POWERED WHEELCHAIR, GP-201 is ITI.

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Other records listing Emg Technology Co., Ltd. as applicant

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Related Devices (Code: ITI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K262582Electric wheelchair (GP100)Suzhou Green Pine Medical Co., Ltd.K262054Electric WheelchairYongkang Joymax Medical Technology Co., Ltd.K260053Power Wheelchair (OS-R-M01I)Beijing OrionStar Technology Co., Ltd.K260229Electric wheelchair (HC819N, HC830N, HC831N)Yongkang Hengyi Vehicle Co., Ltd.K261354Electric wheelchair (D03)Foshan Sowell Medical Technology Co., Ltd.K261149Electric Wheelchair (DY611A-2, DY612A-1)Zhejiang Lumbre Electric Appliance Co., Ltd.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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